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NEWS
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Pharmacy
Quality of pharmaceutical production is put by technology and the manufacture organization, including the cleanliness of technological mediums. Since 2000 Miass Factory of Medical Equipment has carried out designing and construction of cleanrooms for different fields of industries. As the base for this direction of activity 10-years-old experience of our factory in creation of cleanrooms for medical units serves...
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CLEANROOM
- Air treatment, decontamination and distribution system;
- Climate control system;
- Cleanroom structure (structural elements providing leakproofness);
- medical, technological and engineering equipment integrated with the cleanroom structure.
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News
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| АМС МЗМО/English Version/News/05.10.2009 - “AMS”-“MFME” again confirms quality
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“AMS”-“MFME” again confirms quality
 Within the limits of the regular surveillance audit which has taken place from September, 30th till October, 1st, the commission of certification center Autonomus Noncommercial Organization "International Quality Systems Center" (Chelyabinsk) including experts But A.N. and Dolmatov A.S., spent check of conformity of quality management system of the enterprise to requirements of the new standard - GOST R ISО 9001-2008. Till 2009 at the enterprise the certificate of conformity to the standard of GOST R ISО 9001-2001 operated.
According to the head of department of a quality management Galina Aleksandrovna Novokreshchenova, release of qualitative production is priority for the enterprise that demands conformity of all processes of quality management system to the international standards. Main objectives of surveillance audit - acknowledgement of conformity of a quality management system of the enterprise to requirements of the standard by check of processes QMS, revealing of areas for improvement and delivery necessary for it recommendations.
As a result of auditor’s check the high level of conformity of QMS processes has been noted. The quality management system of the enterprise corresponds to all requirements of GOST R ISО 9001-2008. The certified commission recommended to the center to make on certification the decision on "АМS" - "МFМE" delivery of the certificate of conformity QMS to requirements of GOST R ISО 9001-2008 with period of validity 3 years. This certificate confirms meeting all the requirements of this standard with reference to designing, working out, manufacture, delivery, carrying out of assembly and starting-up and adjustment works and certification, to repair and service: the medical equipment, complexes of pure and especially pure premises for electronic, food, medical, microbiological and a pharmaceutical industry and medical institutions
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